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Low Frequency TMS on DLPFC and OFC in OCD Patients

Comparative Study of the Therapeutic Effect of Low Frequency TMS on DLPFC and OFC in OCD Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03207633
Enrollment
60
Registered
2017-07-05
Start date
2017-07-01
Completion date
2018-07-30
Last updated
2020-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychiatric Disorder

Keywords

OCD, rTMS, right orbitofrontal cortex

Brief summary

This study aims to evaluate the therapeutic effect of low frequency rTMS over the right DLPFC, versus right OFC versus Sham group of obsessive-compulsive disorder (OCD) patients. Sixty patients will be recruited from the out-patient psychiatric clinic of a university hospital, and randomized into three equal groups. The 1st group will receive 10 sessions of low frequency rTMS targeting right DLPFC by means of a butterfly coil, 120% RMT, 1 Hz, 3 trains, each of 500 pulses with a 40 seconds inter-train interval allowing the coil to cool. The 2nd group will receive 10 sessions of low-frequency rTMS over the right orbitofrontal cortex (OFC), the international 10-20 EEG system will be used to position the coil over the right OFC, at the right frontopolar 2 (Fp2) electrode site, using the following parameters: 120% motor threshold, 1 Hz, 3 trains, each of 500 pulses with a 40 seconds inter-train interval allowing the coil to cool. The 3rd group will receive sham stimulations with the same pulse delivery as the other groups but with the coil placed perpendicular to the scalp. The resting motor threshold (RMT) and cortical silent period (CSP) at different intensities from 110 % to 150 % will be measured before and after the end of sessions. All assessments like (Y-BOCS), (HAM-A), Beck Depression Inventory, (CGI-S), (MoCA) will be performed before and after end of the sessions and 3 months later.

Detailed description

This study aims to evaluate the therapeutic effect of low frequency rTMS over the right DLPFC, versus right OFC versus Sham group of OCD patients. Sixty patients will be recruited from the out-patient psychiatric clinic of a university hospital, the patients will be randomized into three groups (20 patients for each group) using closed envelopes. The first group (20 patients) will receive 10 sessions of low frequency rTMS targeting right DLPFC by means of a Butterfly coil, The DLPFC stimulation site was defined as the region 5 cm dorsolateral in the same sagittal plane as the optimal site for MT production in the first dorsal interosseous, using the following parameters: 120% RMT, 1 Hz, 3 trains, each of 500 pulses with a 40 seconds inter-train interval allowing the coil to cool. The second group (20 patients) will receive 10 sessions of low-frequency rTMS over the right orbitofrontal cortex (OFC) by means of a butterfly coil, the international 10-20 EEG system will be used to position the coil over the right OFC, at the right frontopolar 2 (Fp2) electrode site, using the following parameters: 120% motor threshold, 1 Hz, 3 trains, each of 500 pulses with a 40 seconds inter-train interval allowing the coil to cool. The third group (the sham condition) (20 patients) group will receive sham stimulations with the same pulse delivery as the other groups but with the coil placed perpendicular to the scalp. The resting motor threshold (RMT) and cortical silent period (CSP) at different intensities from 110 % to 150 % will be measured before and after the end of sessions. All assessments like (Y-BOCS), (HAM-A), Beck Depression Inventory, (CGI-S), (MoCA) will be performed before and after end of the sessions and 3 months later.

Interventions

PROCEDURERepetitive trans-magnetic stimulation (rTMS) on DLPFC

Repetitive trans-magnetic stimulation (rTMS) on DLPFC

PROCEDURERepetitive trans-magnetic stimulation (rTMS) on OFC

Repetitive trans-magnetic stimulation (rTMS) on OFC

PROCEDURESham repetitive trans-magnetic stimulation (rTMS)

Sham repetitive trans-magnetic stimulation (rTMS)

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* being 18 or over * being assigned a Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) or DSM-V diagnosis of OCD by the referring psychiatrist

Exclusion criteria

* (1) presenting established cognitive or communication problems which makes it challenging to understand the questionnaires and take part in the therapeutic encounters * (2) suffering from other severe psychiatric disorders, metabolic, or neurological disorders . * (3) Patients with pacemaker, or metallic devices

Design outcomes

Primary

MeasureTime frameDescription
Yale-Brown Obsessive Compulsive Scale (Y-BOCS)Three monthsAssessment of Obsessive Compulsive disorder using (Y-BOCS)
Hamilton Anxiety Rating Scale (HAM-A)Three monthsAssessment of anxiety using Hamilton scale
Beck Depression InventoryThree monthsAssessment of Depression using Beck depression inventory
Clinical Global Impression-Severity scale (CGI-S)Three monthsAssessment of clinical severity using CGI-S
Montreal Cognitive Assessment (MoCA)Three monthsAssessment of cognitive function using (MoCA)

Secondary

MeasureTime frameDescription
Changes of cortical excitability parameters (RMT and CSP)Ten daysMeasurment of changes of cortical excitability parameters (RMT and CSP) before and after sessions in the three groups.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026